WordNet

not direct in spatial dimension; not leading by a straight line or course to a destination; "sometimes taking an indirect path saves time"; "you must take an indirect course in sailing"
extended senses; not direct in manner or language or behavior or action; "making indirect but legitimate inquiries"; "an indirect insult"; "doubtless they had some indirect purpose in mind"; "though his methods are indirect they are not dishonest"; "known as a shady indirect fellow"
having intervening factors or persons or influences; "reflection from the ceiling provided a soft indirect light"; "indirect evidence"; "an indirect cause"
not as a direct effect or consequence; "indirect benefits"; "an indirect advantage"
abnormally high amounts of bile pigment (bilirubin) in the blood

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Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindred.

Houston BL, Zelinski T, Israels SJ, Coghlan G, Chodirker BN, Gallagher PG, Houston DS, Zarychanski R.SourceUniversity of Manitoba, Winnipeg, Canada.
Blood cells, molecules & diseases.Blood Cells Mol Dis.2011 Dec 15;47(4):226-31. doi: 10.1016/j.bcmd.2011.08.001. Epub 2011 Sep 25.
The hereditary stomatocytoses are a group of heterogeneous conditions associated with chronic red cell hemolysis for which the causative genetic mutations are not known. We investigated 137 members of a large Canadian kindred with phenotypic findings consistent with hereditary xerocytosis, one of th
PMID 21944700

Fretzayas A, Moustaki M, Liapi O, Karpathios T.Source3rd Department of Pediatrics, "Attikon" University Hospital, Athens University, School of Medicine, 1 Rimini str, Haidari, 12462, Athens, Greece, mar.moustaki@gmail.com.
European journal of pediatrics.Eur J Pediatr.2011 Dec 9. [Epub ahead of print]
Gilbert syndrome is a common autosomal dominant hereditary condition with incomplete penetrance and characterized by intermittent unconjugated hyperbilirubinemia in the absence of hepatocellular disease or hemolysis. In patients with Gilbert syndrome, uridine diphosphate-glucuronyl transferase activ
PMID 22160004

綾田穣,石川哲也,奥村明彦,堀田直樹,広瀬昭憲,増子和郎,各務伸一
肝臓 50(3), 139-144, 2009-03-25
症例は，56歳女性．心窩部痛と嘔吐に対し市販薬を内服するも改善せず，外来を受診．黄疸，肝胆道系酵素の上昇を認めたため入院となった．市販薬による薬物性肝障害を疑い，内服を中止．肝障害は軽快した．退院後，高脂血症に対しフルバスタチンナトリウムを投与したところ再び肝障害が出現した．内服中止により，肝障害は改善したが，以後も持続する間接ビリルビン優位の高ビリルビン血症を認めた．Gilbert症候群を疑い， …
NAID 10024804922

Temporary Hyperbilirubinemia in Two Patients During Treatment for Idiopathic Nephrotic Syndrome

Liang Lijun,リャンリジュン,梁麗俊
山形大学紀要. 医学 : 山形医学 = Bulletin of the Yamagata University. Medical science : Yamagata medical journal 22(1), 41-44, 2004-02-16
… We present two patients with idiopathic nephrotic syndrome who showed temporary indirect hyperbilirubinemia during the course of treatment with immunosuppressant drugs and/or steroids. … Hyperbilirubinemia should be considered as one of the adverse effects of immunosuppressant drugs and/or steroids in patients carrying the polymorphic mutations of the B-UGT gene. … Key words : nephrotic syndrome, bilirubin uridine-diphosphate glucuronosyltransferase, hyperbilirubinemia …
NAID 120001717471